N-t-butoxycarbonyl protection of primary and secondary amines in the hydroboration reaction: Synthesis of amino alcohols

Article abstract of DOI:10.1080/00397919508015894

The use of the BOC group as a protecting group in the hydroboration of aminoalkenes is described. The isolated yields of amino alcohols via the hydroboration-oxidation sequence are excellent.

Full text of DOI:10.1080/00397919508015894

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Synthetic Communications: An
International Journal for Rapid
Communication of Synthetic
Organic Chemistry
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N-t-Butoxycarbonyl Protection
of Primary and Secondary
Amines in the Hydroboration
Reaction: Synthesis of Amino
Alcohols
George W. Kabalka a , Nan-Sheng Li a & R. David
Pace a
a Departments of Chemistry and Radiology, The
University of Tennessee, Knoxville, TN, 37996-1600
Published online: 23 Sep 2006.
To cite this article: George W. Kabalka , Nan-Sheng Li & R. David Pace (1995): N-t-
Butoxycarbonyl Protection of Primary and Secondary Amines in the Hydroboration
Reaction: Synthesis of Amino Alcohols, Synthetic Communications: An International
Journal for Rapid Communication of Synthetic Organic Chemistry, 25:14, 2135-2143
To link to this article: http://dx.doi.org/10.1080/00397919508015894
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